Canonical Allele Identifier: CA504024947
Gene: MIR122HG HGNC NCBI

Linked Data

gnomAD v4: 18-58449608-T-C
MyVariant Identifiers: chr18:g.56116840T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.58449608T>C , CM000680.2:g.58449608T>C GRCh38
NC_000018.9:g.56116840T>C , CM000680.1:g.56116840T>C GRCh37
NC_000018.8:g.54267820T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753465.2:n.847T>C
NR_170243.1:n.307+68T>C
NR_170244.1:n.307+68T>C
NR_170245.1:n.307+68T>C
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